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Conduct and medical supervision of clinical studies including pre-, during and post trial activities (fe general monitoring, safety follow up, medical data review, scientific support and presentations, investigator meetings



Current Experience

  • Consultant Medical manager
    Since February 2016
    Consultant Clincical Research Physician, responsible for conduct and medical supervision of clinical trials in Oncology

Past Experience

  • Study responsible physician
    September 2007 --- February 2016
    Responsible for the conduct and medical monitoring of clinical trials in HIV/HCV

  • Medical Liaison Manager
    January 2007 --- June 2007
    medical liaison manager in multiple sclerosis domain

  • Country Study Manager
    April 2003 --- December 2006
    Outsourced via CRA Belgium Responsible for project management, conduct and medical monitoring of oncology studies

  • Senior Clinical Research Associate (CRA)
    September 1998 --- March 2003
    Outsourced at Pfizer and Merckle . Responsible for conduct and mecial monitoring of clinical studies in the urology and osteoporosis domain

  • Clinical Research Physician
    June 1996 --- October 1998
    Outsourced via Quintiles . Responsible for Conduct and medical supervision of clinical study in cardiovascular domain

  • Clinical Research Associate (CRA)
    September 1992 --- June 1996
    Monitoring ,conduct and medical supervison of clinical studies in infectiology and diabetology domain


Self Assessment :
CommunicativeCreative thinkingFlexibilityProactivitySelf-confidenceOptimismInterest in knowledgeProblem solving


LinkedIn Assessment :
oncologyClinical researchClinical trialsPharmaceutical IndustryClinical DevelopmentGood Clinical Practice (GCP)Infectious diseasesMedicineCRO managementClinical Trial Management System (CTMS)Life SciencesDrug DevelopmentGCP

Skills and Expertise

Self Assessment :
Assure medical quality Interact with physicians Interact with nurses Monitor a clinical study Search literature on clinical trialsApprove patient informationApprove consent documentsAssess subject safetyAssist with site trainingAttend investigator meetingCommunicate with investigatorConduct literature searchesConfirm protocol compliancecontrol different protocol versions and other essential documentsCreate clinical project documents according to the protocolDevelop training materialsInteract with CROsInteract with KOLInteract with nursesManage subject safetyMonitor dataOral presentationParticipate in medical reviewProvide medical insightsProvide trainingRead medical literature to maintain current awareness and knowledgeUpdate Clinical Trials Management System (CTMS) Work cross-functionally


  • Medical doctor in medicine from Ghent University in 1990


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Professional Proficiency

Work Preferences

  • Positions I am interested in:
    Medical Study responsible physician
  • Positions I am NOT interested in:
  • Locations I am interested in:
  • Work From Home:
    Yes, 1 Days
  • Work Regime:
    BrightOwl freelancer :    32 Hours per week
  • International:
  • Availability:
    Apr 2018 : 80%
    May 2018 : 80%
    Jun 2018 : 80%
    Jul 2018 : 80%

Area / Region



Driving License
  • Yes